Ref #: 33739

Employment type: Permanent - Full-Time

Location: Chennai, Bangalore and Home based

Posted: 15-Nov-2021



Participate in the lifecycle of producing key data and/or reports in support of data review reporting
development including evaluation of requirements, design specifications, interface to
programmers, report programming, coordinate validation and rollout activities along with providing
quantitative analytical support. These tasks are to be performed independently or team based with
minimal guidance and supervision.

Job Title : Senior/Principal Report Programmer
Job location : Chennai /Bangalore
Both - Home based /Office based
No of years of experience: 5 to 7+ years of relevant exp in Jreview, report writing and SAS Skills
Salary : As per Industry standards with attractive benefits
Skill set : Strong knowledge of programming practices and concepts (including data sources,
transformation, tools, languages and processes). Proficiency in SAS (required), and R, Python
experience is optional.
Experience in using tools intended for report writing, analytics, visualizations, or dashboard
creation such as Spotfire, Tableau, Qlik, JReview, Business Objects, Oracle BI or Crystal Reports
a plus.
Fluent in English, both written and oral

Solid understanding of Clinical Data Standards CDISC SDTM
Strong understanding of relational databases (including RAVE) and industry standard data models
are required.
Able to communicate technical information in a non-technical fashion.
Proven proficiencies in project management.
Ability to successfully manage multiple tasks and timelines.
Able to work independently and in a team environment.
Ability to liaise professionally with stakeholders
Understanding of Drug Development Process, ICH-GCP, CDISC standards and Health Authority
guidelines and regulations.
Inspire new and creative ways to meet data review objectives through proactive identification of
gaps, inefficiencies in current processes and projects recommending opportunities for

Proactively engage in project team meetings, lead and organize meetings to develop detailed plans and
as applicable.
Partner with functional experts to translate requirements for data and reporting solutions creating
standardized, replicable outputs and visualizations for self and programming teams.
Analyze data sources, design and execute data reports (including validation), visualizations through
understanding and translation of business requirements.
Provide hands on SAS programming, data manipulation for all aspects of data quality and clinical safety
review reports.

University or college degree in Life Sciences, Mathematics, Computer Science, MedicaI Informatics or equivalent degree

Why join the DOCS team at ICON?

Working at ICON is more than a job, it’s a calling for people who care and are passionate about improving patients’ lives. At ICON, we care about our people and your passion, you are key to our success. We aim to provide an open and friendly work environment where we empower our people and provide them with opportunities to develop their long-term career.

At ICON you will have the opportunity to work with one of the global top 20 pharmaceutical companies, working on novel therapies that deliver real impact. If you want a career with a difference, ICON is the place for you.

#SASJob or #Clinical SAS Programmer or #Reports #Jreview